University of Notre Dame
Browse

File(s) stored somewhere else

Please note: Linked content is NOT stored on University of Notre Dame and we can't guarantee its availability, quality, security or accept any liability.

Methods for the visualization and analysis of extracellular matrix protein structure and degradation

journal contribution
posted on 2018-08-23, 00:00 authored by Annemarie K. Leonard, Elizabeth A. Loughran, Kevin McAbee, Sharon StackSharon Stack, Marwa Asem, Matthew J RavosaMatthew J Ravosa, Oleg Kim, Yueying LiuYueying Liu, Yuliya KlymenkoYuliya Klymenko
This chapter highlights methods for visualization and analysis of extracellular matrix (ECM) proteins, with particular emphasis on collagen type I, the most abundant protein in mammals. Protocols described range from advanced imaging of complex in vivo matrices to simple biochemical analysis of individual ECM proteins. The first section of this chapter describes common methods to image ECM components and includes protocols for second harmonic generation, scanning electron microscopy, and several histological methods of ECM localization and degradation analysis, including immunohistochemistry, Trichrome staining, and in situ zymography. The second section of this chapter details both a common transwell invasion assay and a novel live imaging method to investigate cellular behavior with respect to collagen and other ECM proteins of interest. The final section consists of common electrophoresis-based biochemical methods that are used in analysis of ECM proteins. Use of the methods described herein will enable researchers to gain a greater understanding of the role of ECM structure and degradation in development and matrix-related diseases such as cancer and connective tissue disorders.

History

Date Modified

2018-10-12

Language

  • English

Usage metrics

    Integrated Imaging Facility

    Categories

    No categories selected

    Keywords

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC